MeSH Browser

MeSH Supplementary: Spinocerebellar ataxia 27
Unique ID: C537204
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537204
Entry Term(s): Cerebellar ataxia, autosomal dominant, FGF14-related; Nystagmus 4, congenital, autosomal dominant; SCA27 Spinocerebellar ataxia 27; SCA27A; Spinocerebellar ataxia 27A; Vestibulocerebellar disorder with predominant ocular signs
Registry Numbers: 0
Heading Mapped to: *Spinocerebellar Degenerations
Frequency: 10
Date of Entry: 2024/11/05
Revision Date: 2024/11/05

Spinocerebellar ataxia 27 MeSH Supplementary Concept Data 2025